PrimePCR™ SYBR® Green Assay: DLGAP1, Human

PrimePCR Primer Assays for Real-Time PCR oligo primer pair tube for SYBR Green gene expression

Real-time PCR primer assay designed for SYBR® Green gene expression analysis.

Info:   Recommended - best coverage; Same primer pair as used in probe assay qHsaCEP0053979

List Price:    $174.00
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Assay Information

Technology:   qPCR
Assay Type:   SYBR® Green
Application:   Gene Expression
Unique Assay ID:   qHsaCED0046718
Assay Design:   exonic
Chromosome Location:   18:3534370-3534471question
Amplicon Length:   72
Splice Variants Targeted:   ENST00000400147 ENST00000400149 ENST00000400155 ENST00000400150 ENST00000315677 ENST00000534970 ENST00000539435 ENST00000581699 ENST00000400145 ENST00000581527 ENST00000584874 ENST00000515196

Gene Information

Description Not Available

Gene Symbol:   DLGAP1
Gene Name:   discs, large (Drosophila) homolog-associated protein 1
Aliases:   DAP-1, DAP-1-ALPHA, DAP-1-BETA, GKAP, MGC88156, SAPAP1, hGKAP
RefSeq:   NC_000018.9 NT_010859.14
Ensembl:   ENSG00000170579
Entrez:   9229
Chromosome Mapping:   18p11.3

The below validation information is for the Primer Pair only   Download Validation Data (.pdf)


Products used to generate validation data:

Real-Time PCR Instrument CFX384 Real-Time PCR Detection System
Reverse Transcription Reagent iScript™ Advanced cDNA Synthesis Kit for RT-qPCR
Real-Time PCR Supermix SsoAdvanced™ Universal SYBR® Green Supermix
Experimental Sample qPCR Human Reference Total RNA

Summary Data:

R2 0.998700
y-intercept 36.840000
Efficiency 92

Amplification Plot
Amplification of cDNA generated from universal RNA.

Amplification of cDNA generated from universal RNA.

Melt Peak
Melt curve analysis of above amplification.

Melt curve analysis of above amplification.

Standard Curve
Standard curve generated using 20 million copies of template diluted 10 fold to 20 copies.

Standard curve generated using 20 million copies of template diluted 10 fold to 20 copies.

Number Description Download
10039761 PrimePCR™ Assays Quick Guide, Ver B Click to download